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M. Hervieu

Publications and source records attributed to M. Hervieu.

At least 19 recordsLinked to original sources

The magnetoresistive behavior of Cr-doped manganites Pr0.44Sr0.56MnO3

A complex structural, magnetic and electric transport investigation shows that the Cr doping on Mn sites in the A-type antiferromagnet Pr0.44Sr0.56MnO3 provokes a non-uniform magnetic state with coexisting FM and AFM regions. Irrespective of the ratio of magnetic phases, the samples exhibit a non-metallic behavior of resistivity and thermopower, pointing to the nanoscopic nature of the phase separation. A particularly large magnetoresistance encountered in a broad range of temperatures for samples with Cr doping of 4 - 6 % supports such idea.

cond-mat.mtrl-sci

Structure determination of a brownmillerite Ca2Co2O5 thin film by Precession Electron Diffraction

Calcium cobaltite thin films with a ratio Ca/Co=1 were grown on (101)-NdGaO3 substrate by the pulsed laser deposition technique. The structure of the deposited metastable phase is solved using a precession electron diffraction 3D dataset recorded from a cross-sectional sample. It is shown that an ordered oxygen-deficient Ca2Co2O5+d perovskite of the brownmillerite-type with lattice parameters a= 0.546nm, b=1.488nm and c=0.546nm (SG: Ibm2) has been stabilized using the substrate induced strain. The structure and microstructure of this metastable cobaltite is further discussed and compared to related bulk materials based on our transmission electron microscopy investigations

cond-mat.mtrl-sci

Magnetic states and spin-glass properties in Bi0.67Ca0.33MnO3: macroscopic ac measurements and neutron scattering

We report on the magnetic properties of the manganite Bi_{1-x}Ca_{x}MnO_3 (x=0.33) at low temperature. The analysis of the field expansion of the ac susceptibility and the observation of aging properties make clear that a spin glass phase appears below T = 39K, in the presence of magnetic order. Neutron scattering shows both magnetic Bragg scattering and magnetic diffusion at small angles, and confirms this coexistence. In contrast to Pr_{1-x}Ca_{x}MnO_3 (x=0.3-0.33) which exhibits a mesoscopic phase separation responsible for a field driven percolation, the glassy and short range ferromagnetic order observed here does not cause colossal magnetoresistance (CMR).

cond-mat.mtrl-sci

Absence of long-range Ni/Mn ordering in ferromagnetic La2NiMnO6 thin films

Epitaxial La2NiMnO6 thin films have been grown on (001)-oriented SrTiO3 using the PLD technique. The thin films are semiconducting and FM with a TC close to 270K, a coercive field of 920Oe, and a saturation magnetization of 5muB per f.u. TEM, conducted at RT, reveals a majority phase having "I-centered" structure with a=c=1.4asub and b=2asub along with a minority phase-domains having "P-type" structure (asub being the lattice parameter of the perovskite structure). A discusion on the presence of Ni/Mn long-range ordering, in light of recent literature on double perovskites La2NiMnO6 is presented.

cond-mat.mtrl-sci

Structural phase transition and magnetism in hexagonal srmno

The structural and magnetic properties of the hexagonal four-layer form of SrMnO$_3$ have been investigated by combining magnetization measurements, electron diffraction and high-resolution synchrotron X-ray and neutron powder diffraction. Below 350K, there is subtle structural phase transition from hexagonal symmetry (space group $P6_3/mmc$) to orthorhombic symmetry (space group $C222_1$) where the hexagonal metric is preserved. The second-order phase transition involves a slight tilting of the corner-sharing Mn$_{2}$O$_{9}$ units composed of 2 face-sharing MnO$_6$ octahedra and the associated displacement of Sr$^{2+}$ cations. The phase transition is described in terms of symmetry-adapted displacement modes of the high symmetry phase. Upon further cooling, long range magnetic order with propagation vector $\mathbf{k}=(0,0,0)$ sets in below 300K. The antiferromagnetic structure, analyzed using representation theory, shows a considerably reduced magnetic moment indicating the crucial role played by direct exchange between Mn centers of the Mn$_{2}$O$_{9}$ units.

cond-mat.str-el

Enhancement of giant magnetoresistance effect in the Ruddlesden-Popper phase Sr3Fe2-xCoxO7-d: Predominant role of oxygen nonstoichiometry and magnetic phase separation

The magnetic and magnetotransport properties of the Sr3Fe2-xCoxO7-d system (0.2 <= x <= 1.0) were systematically investigated. This oxide system exhibits a giant magnetoresistance (GMR) effect at low temperatures, reaching up to 80% in 7 T at 5 K. Ac-susceptibility measurements show that there exists a strong competition between ferromagnetic (F) and spin glass states, and the balance between these two magnetic states can be controlled by varying cobalt (x) and/or oxygen contents (d). Importantly, the MR effect is closely related to the magnetic property: the development of magnetic disordering leads to enhancement in the negative MR effect. It is suggested that the compound segregates into F clusters embedded in a non-F matrix, being a naturally occurring analog of the artificial granular-GMR materials, as in the doped perovskite cobaltites, La1-xSrxCoO3 (x < 0.18).

cond-mat.str-el

The impact of niobium doping upon the magnetotransport properties of the oxygen-deficient perovskite SrCo1-xNbxO3-d

The oxygen-deficient perovskite cobaltite SrCo1-xNbxO3-d was synthesized by direct solid-state reaction and its magnetotransport properties were investigated. This cobaltite exhibits an unusual ferromagnetic behavior with a transition temperature Tm = 130-150 K and a spin glass like behavior below Tm. Importantly, this phase reaches a large magnetoresistance (MR) value, MR = -(rH - r0) / r0 = 30% at 5 K in 7 T. The large MR effect is believed to be related to the disordered magnetic state induced by the Nb-for-Co substitution.

cond-mat.str-el

Competition between ferromagnetism and spin glass: the key for large magnetoresistance in oxygen deficient perovskites SrCo1-xMxO3-d (M = Nb, Ru)

The magnetic and magnetotransport properties of the oxygen deficient perovskites, SrCo1-xMxO3-d with M = Nb and Ru, were investigated. Both Nb- and Ru-substituted cobaltites are weak ferromagnets, with transition temperatures Tm of 130-150 K and 130-180 K, respectively, and both exhibit a spin glass behavior at temperatures below Tf = 80-90 K. It is demonstrated that there exists a strong competition between ferromagnetism and spin glass state, where Co4+ induces ferromagnetism, whereas Nb or Ru substitution at the cobalt sites induces magnetic disorder, and this particular magnetic behavior is the origin of large negative magnetoresistance of these oxides, reaching up to 30% at 5 K in 7 T. The differences between Nb- and Ru-substituted cobaltites are discussed on the basis of the different electronic configuration of niobium and ruthenium cations.

cond-mat.str-el

Neutron scattering evidence for magnetic field driven abrupt magnetic and structural transitions in a phase separated manganite

Substitutions at the Mn-site of the charge-ordered Pr0.5Ca0.5MnO3 manganite is an effective way to induce abrupt jumps on the magnetic field driven magnetization curve. In order to get new insights into the origin of this remarkable feature, the Pr0.5Ca0.5Mn0.97Ga0.03O3 perovskite manganite has been studied by neutron diffraction, versus temperature and at 2.5K in an applied magnetic field up to 6 Tesla. A weak and complex antiferromagnetic order is found for the low temperature ground-state. Magnetic transitions, associated with structural ones, are evidenced for certain strengths of magnetic field, which gives rise to the step-like behavior corresponding to the magnetization curve. Small angle neutron scattering provides evidence for a nucleation process of micron size ferromagnetic domains which follows the magnetization behavior.

cond-mat.mtrl-sci

Field-Induced Magnetization Steps in Intermetallic Compounds and Manganese Oxides: The Martensitic Scenario

Field-induced magnetization jumps with similar characteristics are observed at low temperature for the intermetallic germanide Gd5Ge4and the mixed-valent manganite Pr0.6Ca0.4Mn0.96Ga0.04O3. We report that the field location -and even the existence- of these jumps depends critically on the magnetic field sweep rate used to record the data. It is proposed that, for both compounds, the martensitic character of their antiferromagnetic-to-ferromagnetic transitions is at the origin of the magnetization steps.

cond-mat.mtrl-sci

Staircase-like metamagnetic transitions in phase-separated manganites: influence of thermal and mechanical treatments

Substitutions in the Mn-sublattice of antiferromagnetic, charge and orbitally ordered manganites was recently found to produce intriguing metamagnetic transitions, consisting of a succession of sharp magnetization steps separated by plateaus. The compounds exhibiting such features can be divided in two categories, depending on whether they are sensitive to thermal cycling effects or not. One compound of each category has been considered in the present study. The paper reports on the influence of two treatments: high-temperature annealing and grinding. It is shown that both of these treatments can drastically affect the phenomenon of magnetization steps. These results provide us with new information about the origin of these jumps in magnetization.

cond-mat.mtrl-sci

Large positive magnetocaloric effect in a perovskite manganite

We investigate the magnetothermodynamic properties of the perovskite manganite Pr0.46Sr0.54MnO3. Our data imply that the paramagnetic to antiferromagnetic transition at TN = 210 K is first order with an abrupt decrease of volume (~ 0.14 % in zero magnetic field) and is accompanied by a sharp anomaly in specific heat. Upon application of a sufficiently large magnetic field, the antiferromagnetic phase transforms into a ferromagnetic phase with a sharp increase in sample volume. This field induced transition results in a large positive magnetocaloric effect just below TN (∆Sm = 10.4 Jkg-1K-1 at H = 5.5 T), which is associated with the increasing stability of the antiferromagnetic state with decreasing temperature.

cond-mat.mtrl-sci

Giant frequency dependence of dynamic freezing in nanocrystalline ferromagnetic LaCo0.5Mn0.5O3

We have investigated the magnetic properties of nanocrystalline LaCo0.5Mn0.5O3. The temperature dependence of the imaginary part of the a.c. susceptibility shows a strongly frequency dependent maximum at a temperature, Tf, which is well below the ferromagnetic transition temperature (TC ~ 230 K). The frequency dependence of Tf obeys the Arrhenius relation, f = foexp(-Ea/kBT), with physically reasonable values of fo = 109 Hz and Ea/kB = 1518 K. The frequency shift of Tf per decade of frequency is one of the highest values observed in any magnetic system, and a similarly large value is also found in LaCo0.4Mg0.1Mn0.5O3, suggesting that such behavior is intrinsic despite the apparent presence of long range ferromagnetic order.

cond-mat.mtrl-sci

Staircase effect in metamagnetic transitions of charge and orbitally ordered manganites

This paper reports on peculiar metamagnetic transitions which take place in antiferromagnetic, charge and orbitally ordered (AFCOO) manganites. At very low temperatures, the virgin magnetization curves of some of these compounds exhibit several, sharp steps giving rise to a staircase-like shape. This staircase effect is shown to be sensitive to various experimental parameters. Several potential interpretations of the staircase effect are discussed in relation to this set of results. A martensitic-like scenario, involving a leading role of the structural distortions associated to the collapse of the orbital ordering, is found to be the most plausible interpretation.

cond-mat.str-el

Relaxor ferromagnetic behavior below the antiferromagnetic transition in La0.5Ca0.5MnO3

A detailed reinvestigation of magnetization in La0.5Ca0.5MnO3 reveals that although a field of H = 7 T applied at T = 5 K after zero field cooling is insufficient to convert the low temperature charge ordered antiferromagnetic phase into ferromagnetic, annealing in a magnetic field as small as H = 1 T induces ferromagnetic clusters in the charge ordered matrix. The volume phase fraction of the ferromagnetic clusters increases nearly linearly with the annealing field until Han = 4 T and then changes dramatically from about 11 % at 5 T to 60 % at Han = 7 T. This is analogous to the field-induced micro to macro polar domains in relaxor ferroelectrics. It is suggested that charge ordered clusters coexist with ferromagnetic phase above the Neel temperature (TN) and these clusters which transform into ferromagnetic by external magnetic fields are supercooled below TN. Our results will be relevant to the observation of many orders of decrease in the resistivity found for H << HC, where HC is the critical field for metamagnetic transition.

cond-mat.mtrl-sci

Ultra-sharp magnetization steps in perovskite manganites

We report a detailed study of step-like metamagnetic transitions in the magnetization and resistivity of polycrystalline Pr0.5Ca0.5Mn0.95Co0.05O3. The steps have a sudden onset below a critical temperature, are extremely sharp (width < 0.2 mT), and occur at critical fields which are linearly dependent on the absolute value of the cooling field in which the sample is prepared. Similar transitions are also observed at low temperature in non-Co doped manganites, including single crystal samples. These data show that the steps are an intrinsic property, qualitatively different from either previously observed higher temperature metamagnetic transitions in the manganites or metamagnetic transitions observed in other materials.

cond-mat.mtrl-sci